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A.I.M. KNOTLESS MENISCAL REPAIR DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K133770
510(k) Type
Traditional
Applicant
ANCHOR INNOVATION MEDICAL (A.I.M.)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/10/2014
Days to Decision
181 days
Submission Type
Summary

A.I.M. KNOTLESS MENISCAL REPAIR DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K133770
510(k) Type
Traditional
Applicant
ANCHOR INNOVATION MEDICAL (A.I.M.)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/10/2014
Days to Decision
181 days
Submission Type
Summary